Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k) Clearances

510(k) cleared devices tracked by MedTracker

HTN 2025-07-11

RipCord

Applicant TriMed, Inc.

K-Number K251134

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FOZ 2025-07-11

BD Cathena Safety IV Catheter

Applicant Becton Dickinson Infusion Therapy Systems, Inc.

K-Number K251155

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EMA 2025-07-11

ResiCem EX

Applicant Shofu Dental Corporation

K-Number K251470

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IYN 2025-07-10

Sonosite LX Ultrasound System

Applicant FUJIFILM Sonosite, Inc.

K-Number K251830

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EIH 2025-07-10

ARENA Star, Galaxy Star

Applicant Arum Dentistry Co., Ltd.

K-Number K250063

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OVD 2025-07-10

CONDUIT SYNFIX Evolution Secured Spacer System

Applicant Avalign Technologies, Inc.

K-Number K250072

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DWF 2025-07-10

RAP Femoral Venous Cannulae

Applicant LivaNova USA, Inc.

K-Number K250283

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KNW 2025-07-10

Marquee Disposable Core Biopsy Instrument and Instrument Kit

Applicant Bard Peripheral Vascular, Inc.

K-Number K250032

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IYN 2025-07-10

Vivid Pioneer

Applicant GE Medical Systems Ultrasound and Primary Care Diagnostics

K-Number K251169

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NFO 2025-07-10

Microcurrent Facial Device (CEC101, EE0101, EEI101)

Applicant Shenzhen Dachi Communication Co., Ltd.

K-Number K244004

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MBI 2025-07-10

Arthrex PushLock Suture Anchors

Applicant Arthrex, Inc.

K-Number K251145

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MRW 2025-07-10

CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant

Applicant Providence Medical Technology, Inc.

K-Number K251885

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